EP2805982B1 - Polybutadiène avec groupes époxy - Google Patents

Polybutadiène avec groupes époxy Download PDF

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Publication number
EP2805982B1
EP2805982B1 EP14167363.2A EP14167363A EP2805982B1 EP 2805982 B1 EP2805982 B1 EP 2805982B1 EP 14167363 A EP14167363 A EP 14167363A EP 2805982 B1 EP2805982 B1 EP 2805982B1
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Prior art keywords
polybutadiene
monomer units
mol
use according
butadiene
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EP14167363.2A
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German (de)
English (en)
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EP2805982A1 (fr
Inventor
Niko HABERKORN
Andreas Berlineanu
Peter Denkinger
Christine BEIERLEIN
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Evonik Operations GmbH
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Evonik Degussa GmbH
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/02—Polycondensates containing more than one epoxy group per molecule
    • C08G59/027—Polycondensates containing more than one epoxy group per molecule obtained by epoxidation of unsaturated precursor, e.g. polymer or monomer
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22—Di-epoxy compounds
    • C08G59/226—Mixtures of di-epoxy compounds

Definitions

  • the present invention relates to the use of a polybutadiene with epoxy groups in a curable composition comprising at least one epoxy resin and at least one curing agent, wherein the polybutadiene is the 1,3-butadiene derived monomer units includes. wherein the proportion of A in the total of the 1,3-butadiene-derived monomer units contained in the polybutadiene is 10 to 60 mol%, and wherein the sum of the proportions of B and C in the entirety of the 1,3-butadiene-derived monomer units contained in the polybutadiene is 40 to 90 mol%. and wherein the epoxy groups have the formula (I) and X represents a linear or branched alkylene group.
  • Polybutadienes are a class of industrially highly-relevant organic compounds produced by the polymerization of 1,3-butadiene available from the cracking of petroleum in large quantities. They are interesting and important starting materials for chemical syntheses equally on a laboratory and large scale.
  • Epoxide groups can be used for a variety of other reactions, especially with anhydrides or amines.
  • the resulting polybutadiene with epoxy groups can thus be reacted with reagents such as diamines to form a durable plastic.
  • Shell Oil Company Research Disclosure, Vol. 416, 12, 1998, page 1594 describes the preparation of butadiene polymers with epoxy groups.
  • the polydiene diols were obtained via anionic polymerization.
  • the poor compatibility of the products and their low functionality of 1.1 or 1.6 and 2 are mentioned.
  • the reaction of the glycidyl ethers with EPICURE 3140 polyamide is described.
  • the invention SU195104 (Rubber Institute Lebedev) describes the synthesis of an anionic polybutadiene polymer to a "living polymer” with metal atoms of the I-III group and their treatment with epichlorohydrin, acids and bases.
  • the "living polymer” is not isolated before the reaction with epichlorohydrin and freed from butadiene oligomers.
  • the products are reacted with maleic anhydride and phthalic anhydride.
  • curable compositions described in the prior art comprising an epoxy resin and a hardener, preferably an amine-containing curing agent, relates to the material properties of the composition which is frequently mechanically stressed in the cured state, in particular the in many cases insufficient impact resistance of the cured compositions.
  • the object underlying the invention is to provide curable compositions.
  • the problem underlying the present invention is solved in a first aspect by using polybutadiene with epoxy groups in a curable composition comprising at least one epoxy resin and at least one curing agent, wherein the polybutadiene is the 1,3-butadiene derived monomer units and includes, wherein the proportion of A in the total of the 1,3-butadiene-derived monomer units contained in the polybutadiene is 10 to 60 mol%, and wherein the sum of the proportions of B and C in the entirety of the 1,3-butadiene-derived monomer units contained in the polybutadiene is 40 to 90 mol%.
  • the problem is solved in one preferred embodiment of the first aspect by a use wherein the proportion of A, B and C on the total of the 1,3-butadiene-derived monomer units contained in the polybutadiene each independently and independently amounts to at least 10%.
  • the problem is solved in a preferred embodiment of the first aspect by a use, wherein the proportion of A on the total of contained in the polybutadiene from 1,3-butadiene derived monomer units 15 to 30, the proportion of B in the entirety of that contained in the polybutadiene From 1,3-butadiene derived monomer units 50 to 70 and the proportion of C in the total of contained in the polybutadiene derived from 1,3-butadiene monomer units is 15 to 30 mol%.
  • the epoxy groups have the formula (I) and X represents a linear or branched alkylene group, preferably a linear alkylene group of the formula - (CH 2 ) x -, where x is 1 to 4, more preferably 1.
  • the problem is solved in a further preferred embodiment of the first aspect by a use, wherein the polybutadiene has 1.5 to 3, preferably 1.75 to 2.5 epoxy groups.
  • the curable composition is a curable composition in adhesive, sealant and acoustic compositions for automotive applications, in cast resin formulations for electrical insulation, in sealants for building materials or for impregnation or bonding of metal, glass and carbon fiber fabrics.
  • the epoxy resin from the group comprising epoxy resins bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, chain extended bisphenol A resins having molecular weights of 700 to 5000, epoxidized novolacs, triglycidyl p-aminophenol, tetraglycidylmethylenedianiline and hexahydrophthalic diglycidyl esters, and cycloaliphatic types.
  • the epoxy resin from the group comprising epoxy resins bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, chain extended bisphenol A resins having molecular weights of 700 to 5000, epoxidized novolacs, triglycidyl p-aminophenol, tetraglycidylmethylenedianiline and hexahydrophthalic diglycidyl esters, and cycloaliphatic types.
  • the at least one curing agent is a hardener selected from the group consisting of amine-containing curing agents having at least two or more primary and / or secondary amino groups or di- and polycarboxylic anhydrides.
  • the hardener is selected from the group comprising substituted ureas, guanamines, guanidines and imidazoles.
  • the problem is solved in a further preferred embodiment of the first aspect by a use, wherein the curing agent is dicyandiamide.
  • the at least one curing agent is a polyamine.
  • the curable composition comprises at least one further compound from the group comprising solvents, reaction accelerators, pigments, fillers, additives, reactive diluents and modifiers.
  • the polybutadiene used according to the invention is a polybutadiene with epoxy groups, the polybutadiene being the monomer units derived from 1,3-butadiene and includes, wherein the proportion of A in the total of the monomer units derived from 1,3-butadiene contained in the polybutadiene is 10 to 60 mol%, and wherein the sum of the proportions of B and C in the entirety of the 1,3-butadiene-derived monomer units contained in the polybutadiene is 40 to 90 mol%.
  • the proportion of A, B and C in the entirety of the monomer units derived from 1,3-butadiene in the polybutadiene is preferably at least and independently of each other at least 10 mol%.
  • the proportion of A in the total of the 1,3-butadiene-derived monomer units contained in the polybutadiene is preferably 15 to 30 mol%
  • the proportion of B in the entirety of the 1,3-butadiene-derived monomer units contained in the polybutadiene is preferably 50 to 70 mol%
  • the proportion of C in the entirety of the monomer units derived from 1,3-butadiene in the polybutadiene is preferably 15 to 30 mol%.
  • the polybutadiene contained in the polybutadiene derived monomer units A), B) and C) also other Be contained monomer units, in particular those which are not derived from 1,3-butadiene.
  • the entirety of the 1,3-butadiene-derived monomer units A), B) and C) contained in the polybutadiene constitutes a proportion of the total of the monomer units incorporated in the polymer, including those derived from 1,3-butadiene and others, of at least 80, preferably 90, more preferably 95, most preferably 100 mole%.
  • the epoxy groups of the polybutadiene having epoxy groups have in particular the formula (I) in which X represents a linear or branched alkylene group, preferably a linear alkylene group of the formula - (CH 2 ) x -, where x is 1 to 4, more preferably 1.
  • the polybutadiene having epoxy groups used according to the invention has, in a preferred embodiment, an average functionality of 1.5 to 3, preferably 1.75 to 2.5. This means in a still preferred embodiment that a polybutadiene molecule, regardless of its length on average 1.5 to 3, preferably 1.75 to 2.5 epoxy groups.
  • the polybutadiene with epoxy groups used according to the invention is almost colorless and has a low viscosity.
  • the viscosity is preferably determined at 20 ° C. using the Haake's rotational viscometer.
  • the provision of the polybutadiene used in accordance with the invention preferably takes place by a process comprising, as step a), the provision of a polybutadiene having hydroxyl groups prepared by free-radical polymerization.
  • a polybutadiene having hydroxy groups can be prepared, for example, by polymerization of 1,3-butadiene in the presence of hydrogen peroxide, water and an organic solvent, as described in U.S. Pat EP12169794.0 is described.
  • polybutadiene as used herein is understood to mean a product obtained by polymerizing monomer units each having at least two conjugated double bonds, in order of increasing preference at least 80, 85, 90, 95, 98, 99 or 99.9% of the monomer units is 1,3-butadiene.
  • the hydroxy-terminated polybutadiene is reacted with a monoepoxy compound in the presence of inert gas.
  • the monoepoxy compound is preferably selected from the group comprising epihalohydrins, preferably epichlorohydrin, ⁇ -methylepichlorohydrin or epibromohydrin, and alkylene oxides, preferably ethylene oxide, 1,2-propylene oxide or 1,2-butylene oxide.
  • epichlorohydrin is used in an amount between 0.5 and 2 moles of epichlorohydrin per equivalent of a polybutadiene-bonded hydroxy group. Particularly preferred is 0.9 to 1.2 moles of epichlorohydrin per equivalent of a polybutadiene bound hydroxy group used.
  • the molar ratio between the monoepoxy compound and the terminal hydroxy groups in the reaction mixture in step b) is 0.5 to 2, preferably 0.9 to 1.2.
  • step b) proceeds in a solvent.
  • the solvent is an aliphatic, such as hexane, heptane, octane, cyclohexane, liquid at room temperature, around an aromatic at room temperature (25 ° C), for example benzene, toluene, one at room temperature liquid esters, for example ethyl acetate, butyl acetate, or to a liquid at room temperature ether, such as diethyl and diisopropyl ether, dioxane and tetrahydrofuran.
  • the type and amount of the solvent depends on the polybutadiene used with hydroxyl groups and the amount of the monoepoxy compound. Solvent mixtures of the solvents mentioned are possible in any proportions. The proportion of the sum of polybutadiene with hydroxy groups and monoepoxy compound in the reaction mixture can be between 5 and 80% by weight in each case.
  • the reaction is preferably carried out in the presence of an inert gas at reduced or elevated pressure.
  • inert gas as used herein means a gas or gas mixture which is inert in its entirety.
  • the inert gas is preferably nitrogen, noble gases or mixtures thereof.
  • step b) lasts for 0.5 to 24 hours.
  • the temperature in step b) is 0 to 150, preferably 0 to 70 ° C.
  • both the polybutadiene with hydroxy groups and the monoepoxy compound can be presented. Alternatively, both compounds can be presented together. Thereafter, the reaction mixture is brought to the reaction temperature by heating.
  • Step b) preferably proceeds in the presence of a metal or semimetal salt as catalyst.
  • a metal or semimetal salt as catalyst. It is at least one metal of the main or subgroups of the periodic table, preferably selected from the group comprising boron, aluminum, zinc and tin, and at least one anion from the group comprising F - , Cl - , BF 4 - , PF 6 - , AsF 6 - , SbF 6 - , ClO 4 - , IO 4 - , and NO 3 -
  • the amount used of the catalyst is preferably between 0.001 to 0.5 moles of the metal salt per equivalent of a polybutadiene bonded hydroxy group. It can be submitted to the reaction components and the catalyst and then reacted.
  • the metal salt catalyst is introduced with the polybutadiene with hydroxy groups and then the monoepoxy compound, preferably epihalohydrin, is added.
  • step c) dehydrohalogenation is carried out by adding at least one alkali metal hydroxide, an alkali metal bicarbonate or an alkali metal carbonate as base to form the alkali metal halide to the reaction mixture from step b).
  • the amount of alkali metal hydroxide added is between 0.7 to 1.4 moles per equivalent hydroxy group bonded to a polybutadiene.
  • the temperature in step c) should be between 0 and 80 ° C.
  • Step b) is preferably carried out in the presence of a solvent and this before, during or after step c), preferably after step c), separated from the reaction mixture.
  • the problem underlying the invention is solved by a composition comprising the above-mentioned polybutadiene with epoxy groups or the polybutadiene having epoxy groups prepared by the aforementioned method and at least one curing agent, optionally additionally at least one epoxy resin.
  • the problem underlying the invention is solved by a binder in adhesive, sealing and acoustic compositions for automotive applications, casting resin formulations for electrical insulation, sealants for building materials, for impregnation or bonding of glass and carbon fiber fabric comprising the aforementioned polybutadiene terminal epoxy groups or the epoxy-terminated polybutadiene prepared by the process described above and at least one curing agent, optionally additionally at least one epoxy resin.
  • the problem underlying the invention is solved by the use of the aforesaid epoxy-terminated polybutadiene or the epoxy-terminated polybutadiene prepared by the previously described process as binders in adhesive, caulking and acoustic compositions for automotive applications, in cast resin formulations for electrical insulation, in sealants for building materials, for impregnation or bonding of glass and carbon fiber fabrics.
  • the problem underlying the invention is solved by a method comprising the step of curing the composition according to the invention.
  • the present invention is based on the surprising finding that polybutadiene with epoxy groups prepared from polybutadiene obtained by means of a free radical polymerization has a low viscosity and glass transition temperature. Without wishing to be bound by any particular theory, the inventors of the present invention suspect that the radical polymerization leads to an anionic polymerization of butadiene to a polybutadiene having a high content of 1,2-vinyl as a monomer on the polymer and that this monomer for those mentioned Properties is causal.
  • the present invention is further based on the surprising discovery that epoxy-terminated polybutadiene, as a constituent of a curable mixture with an epoxy resin and a curing agent, may be suitable for either increasing the toughness of the composition in the cured state or increasing flexibilization in epoxy resins.
  • the present invention relates to the use of a polybutadiene with epoxy groups in curable compositions.
  • a polybutadiene can be obtained from a polybutadiene having hydroxy groups produced by radical polymerization of 1,3-butadiene and then reacting with a monoepoxy compound each comprising the monomer units A), B) and C derived from 1,3-butadiene contained in the polybutadiene ), wherein a square bracket in the chosen in this application formula representation of contained in polybutadiene 1,3-butadiene derived monomer units A), B) and C) shows that provided with the respective square bracket bond not with a methyl group ends, but that the corresponding monomer unit is connected via this bond with another monomer unit or another functional group, in particular a hydroxy group or epoxy group.
  • the monomer units A), B) and C) can be arranged in any order in the polymer. Preferred is a statistical arrangement.
  • the characterization of the mechanical properties of the curable composition of the invention is carried out in the cured state, for example by determining the tensile strength and impact strength (Charpy) of a test specimen according to the test standards DIN 53455 and DIN 53453.
  • the polybutadiene having epoxy groups according to the invention can be used according to the invention in a composition comprising the polybutadiene with epoxy groups and at least one curing agent, optionally additionally at least one epoxy resin.
  • epoxy resin as used herein means a prepolymer having two or more epoxy groups per molecule.
  • crosslinkers also referred to as curing agents.
  • These polymers may be thermosetting and may be in the ranges of, for. B. Civil Engineering (construction), especially in industrial floors, waterproofing and concrete restoration products, composites (fiber composites), potting compounds, paints and adhesives, find use.
  • An overview of the resins and hardeners as well as their use in civil engineering including their properties can be found in H. shoe man, "manual concrete protection by coatings", Expert publishing house 1992, P. 396 -.
  • epoxy resin all epoxy resins in question, which can be cured with amines.
  • the epoxy resins include, for.
  • polyepoxides based on bisphenol A diglycidyl ether bisphenol F diglycidyl ether or cycloaliphatic types such. For example, 3,4-epoxycyclohexyl-epoxyethane or 3,4-epoxycyclohexylmethyl-3,4-epoxy-cyclohexanecarboxylate.
  • At least one epoxy resin is used, which is selected from the group, the epoxy resins based on bisphenol A diglycidyl ether, epoxy resins based on bisphenol F diglycidyl ether and cycloaliphatic types such.
  • the epoxy resins based on bisphenol A diglycidyl ether epoxy resins based on bisphenol F diglycidyl ether and cycloaliphatic types such.
  • 3,4-epoxycyclohexyl-epoxyethane or 3,4-epoxycyclohexylmethyl-3,4-epoxy-cyclohexane-carboxylate, with bisphenol A based epoxy resins and bisphenol F based epoxy resins are particularly preferred.
  • Such compounds are commercially available.
  • the curable composition may comprise more than one epoxy resin according to the invention, ie more than one compound having epoxy groups is present.
  • Suitable hardeners are all hardeners described in the prior art for curable compositions comprising at least one epoxy compound, in particular amine-containing hardeners which have at least two or more primary and / or secondary amino groups, eg. Diethylenetriamine, triethylenetetramine, methylenedianiline, bis (aminocyclohexyl) methane, 3,3'-dimethyl-4,4'-diaminodicyclohexylmethane, tricyclododecanediamine, norbornanediamine, N-aminoethylpiperazine, isophoronediamine, m-phenylenebis (methylamine), 1.3 and / or 1,4-bis (aminomethyl) cyclohexane, Trimethylhexamethylenediamine, polyoxyalkyleneamines, polyaminoamides, and reaction products of amines with acrylonitrile and Mannich bases, furthermore a polyamine selected from the group consisting of isophoronediamine,
  • the hardener used is a compound having at least one anhydride group, preferably a di- or polycarboxylic anhydride.
  • exemplary compounds include trimellitic anhydride adducts and hexahydrophthalic anhydride or methyl-hexahydrophthalic anhydride.
  • the composition according to the invention may comprise further compounds, in particular a solvent, for.
  • a solvent for.
  • at least one reaction accelerator preferably from the group of organic acids or tertiary amines, for.
  • salicylic acid aminoethylpiperazine, tris (N, N-dimethylaminomethyl) phenol, further pigments, fillers and / or additives, a reactive diluent, which is preferably selected from the group of mono-, bi- or polyfunctional, liquid at room temperature epoxy compounds, z.
  • a modifier such as benzyl alcohol, cou
  • Examples 1 to 3 describe the synthesis of polybutadienes having epoxy groups which can be used according to the invention.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)

Claims (11)

  1. Utilisation de polybutadiène contenant des groupes époxy dans une composition durcissable comprenant au moins une résine époxyde et au moins un durcisseur,
    le polybutadiène comprenant les unités monomères dérivées de 1,3-butadiène
    Figure imgb0023
    Figure imgb0024
     et
    Figure imgb0025
     la proportion de A par rapport à la totalité des unités monomères dérivées de 1,3-butadiène contenues dans le polybutadiène étant de 10 à 60 % en moles,
    et la somme des proportions de B et C par rapport à la totalité des unités monomères dérivées de 1,3-butadiène contenues dans le polybutadiène étant de 40 à 90 % en moles,
    et les groupes époxy présentant la formule (I)
    Figure imgb0026
     et X représentant un groupe alkylène linéaire ou ramifié.
  2. Utilisation selon la revendication 1, dans laquelle les proportions de A, B et C par rapport à la totalité des unités monomères dérivées de 1,3-butadiène contenues dans le polybutadiène sont chacune et indépendamment les unes des autres d'au moins 10 %.
  3. Utilisation selon l'une quelconque des revendications 1 à 2, dans laquelle la proportion de A par rapport à la totalité des unités monomères dérivées de 1,3-butadiène contenues dans le polybutadiène est de 15 à 30, la proportion de B par rapport à la totalité des unités monomères dérivées de 1,3-butadiène contenues dans le polybutadiène est de 50 à 70, et la proportion de C par rapport à la totalité des unités monomères dérivées de 1,3-butadiène contenues dans le polybutadiène est de 15 à 30 % en moles.
  4. Utilisation selon l'une quelconque des revendications 1 à 3, dans laquelle le polybutadiène comprend 1,5 à 3, de préférence 1,75 à 2,5 groupes époxy.
  5. Utilisation selon l'une quelconque des revendications 1 à 4, dans laquelle la composition durcissable est une composition durcissable dans des masses adhésives, d'étanchéité et acoustiques pour des applications automobiles, des formulations de résines à couler pour l'isolation électrique, des masses d'étanchéité pour matériaux de construction, pour l'imprégnation ou le collage de métaux, de tissus en fibres de verre et de carbone.
  6. Utilisation selon l'une quelconque des revendications 1 à 5, dans laquelle la résine époxyde est choisie dans le groupe comprenant les résines époxydes à base d'éther diglycidylique de bisphénol A, d'éther diglycidylique de bisphénol F, les résines de bisphénol A à chaîne allongée ayant des masses molaires de 700 à 5000, les novolaques époxydées, le triglycidyl-p-aminophénol, la tétraglycidyl-méthylène-dianiline et l'ester diglycidylique de l'acide hexahydrophtalique et les types cycloaliphatiques.
  7. Utilisation selon l'une quelconque des revendications 1 à 6, dans laquelle ledit au moins un durcisseur est un durcisseur qui est choisi dans le groupe comprenant les durcisseurs aminés contenant au moins deux groupes amino primaires et/ou secondaires ou plus, les anhydrides d'acides di- et polycarboxyliques.
  8. Utilisation selon l'une quelconque des revendications 1 à 6, dans laquelle le durcisseur est choisi dans le groupe comprenant les urées substituées, les guanamines, les guanidines et les imidazoles.
  9. Utilisation selon la revendication 8, dans laquelle le durcisseur est le dicyandiamide.
  10. Utilisation selon la revendication 7, dans laquelle ledit au moins un durcisseur est une polyamine.
  11. Utilisation selon l'une quelconque des revendications 1 à 10, dans laquelle la composition durcissable comprend au moins un composé supplémentaire du groupe comprenant les solvants, les accélérateurs de réaction, les pigments, les charges, les additifs, les diluants réactifs et les modificateurs.
EP14167363.2A 2013-05-24 2014-05-07 Polybutadiène avec groupes époxy Not-in-force EP2805982B1 (fr)

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EP13169194.1A EP2805981A1 (fr) 2013-05-24 2013-05-24 Polybutadiène avec groupes époxides
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JP6657385B2 (ja) * 2015-09-22 2020-03-04 エメラルド・スペシャルティ・ポリマーズ・エルエルシーＥｍｅｒａｌｄ Ｓｐｅｃｉａｌｔｙ Ｐｏｌｙｍｅｒｓ，Ｌｌｃ エポキシ末端ブタジエン及びブタジエンアクリロニトリルコポリマー

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DE2911243A1 (de) * 1979-03-22 1980-10-02 Basf Ag Verfahren zur herstellung kationischer bindemittel und deren verwendung
WO1997048749A1 (fr) * 1996-06-17 1997-12-24 Daicel Chemical Industries, Ltd. Polyene epoxyde, composition de resine epoxy et produit resultant de son durcissement, et materiau de revetement pulverulent
DE10163783A1 (de) * 2001-12-22 2003-07-03 Degussa Verfahren zur Herstellung epoxidierter Polyalkenylene und Verwendung von Phosphonsäuren und deren Derivaten als Katalysator
CN101880514B (zh) * 2010-06-28 2012-06-27 深圳市库泰克电子材料技术有限公司 返修性能好的单组份底部填充胶及其制备方法

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